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The performance of electrochemical glucose oxidation has been overestimated due to a lack of understanding of the interactions between the catalyst surface and glucose. Herein, we unravel the mechanisms of glucose oxidation using atomically well-defined Au25 nanoclusters, exhibiting exceptional activity while maintaining structural integrity. The oxidation reactivity is significantly influenced by applied potential and accordingly altered chemical state of the Au surface, with three distinct mechanisms leading to dominance at different potential regions: an aerobic oxidation pathway near open-circuit, a 1e– electrocatalytic pathway prevailing at low potentials, and a typical 2e– electrocatalytic pathway dominating at higher potentials. The aerobic pathway involves coupling glucose oxidation with an O2 reduction, producing gluconic acid and H2O2, respectively, without an applied potential. In the 1e– pathway, the α-hydrogen of glucose is stripped by the Au surface, resulting in a simultaneous production of gluconic acid and H2 at the anode. Unveiling these pathways enabled the precise evaluation of performance as 100% Faraday efficiency across all potential ranges. Our findings provide a definitive framework for elucidating the structure–activity relationship in the electrocatalysis of biomass.
Seong et al. (Fri,) studied this question.